PTEN NM_000314.8(PTEN):c.176C>G (p.Ser59Ter)

CI-VAR-00061980Explore in graph →p.Ser59TerNM_000314.8:c.176C>GClinVar 404151 rs1060500116

Curated evidence

Evidence by cancer (0 items)

Grouped by cancer context first, then therapy. The same variant can be sensitizing in one cancer and irrelevant in another — contexts are never merged. 50 items per page; a cancer group may continue on the next page.

Data not yet available

No curated evidence item references this variant yet.

ClinVar

Clinical significance (1)

ClinVar interpretations are shown as structured records — significance, review status, star rating, conditions — never flattened into one word.

clinvarCurated1 interpretation · review status and star rating as assigned by ClinVar.

Variation	Clinical significance	Review status	Stars	Conditions	Origin	Submitters	Last evaluated	Source
404151	Pathogenic	criteria provided, multiple submitters, no conflicts	2	PTEN hamartoma tumor syndrome; Hereditary cancer-predisposing syndrome; Cowden syndrome 1; Macrocephaly-autism syndrome; Familial prostate cancer; Glioma susceptibility 2; Familial meningioma; PTEN-related disorder	germline	5	Sep 04, 2024	clinvar